Pullio Hand Sanitizing Wipes Lavender by YES SALES / NAICO Drug Facts

Pullio Hand Sanitizing Wipes Lavender by

Drug Labeling and Warnings

Pullio Hand Sanitizing Wipes Lavender by is a Otc medication manufactured, distributed, or labeled by YES SALES, NAICO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PULLIO HAND SANITIZING WIPES LAVENDER- benzalkonium chloride cloth 
YES SALES

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Drug Facts

ACTIVE INGREDIENT

Benzalkonium Chloride 0.13%

INACTIVE INGREDIENTS

Water, Glycerin, Sodium Benzoate, Ethylhexylglycerin, Polysorbate20, Lavandula Angustifolia(Lavender) Extract, Butylene Glycol,1,2-Hexanediol
,Disodium EDTA, Citric Acid, Tocopheryl Acetate,Fragrance

PURPOSE

Antiseptic

WARNINGS

For external use only
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Stop use and ask a doctor if
■ hypersensitivity symptoms such as erythema, itching and dermatitis happen
■ skin irritation happens
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Do not use
■ in combination with soap or antibacterial cleansing agents
■ the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin
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When using this product
■ aviod using repeatedly in the same area, skin irritation may occur
■ avoid getting into the eyes (if contact occurs, wash well with clean water)
■ if following abnormal symptoms persist, discontinue use :
Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Uses

■ Instant hand antiseptic to decrease bacteria on the skin

Directions

■ Clean with wipes and let dry
■ Do not flush

Other information

■ Read the directions and warnings before use
■ Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PULLIO HAND SANITIZING WIPES LAVENDER 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80618-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80618-020-01	60 g in 1 PACKET; Type 0: Not a Combination Product	09/01/2020	11/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/01/2020	11/30/2020

Labeler - YES SALES (080733755)

Registrant - YES SALES (080733755)

Establishment
Name	Address	ID/FEI	Business Operations
NAICO		694725335	manufacture(80618-020)

Revised: 1/2025

Document Id: 2b05bc3b-86cf-20ca-e063-6394a90a3dfa

34390-5

Set id: fc5816ce-627a-4199-9534-b6a735518aa7

Version: 2

Effective Time: 20250106